These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

250 related articles for article (PubMed ID: 26620033)

  • 1. A Rare Case of Metachromatic Leukodystrophy Confirmed by Arylsulfatase A.
    Alam ST; Akhter S; Rahman MM; Islam KA; Siddique R; Helaly L; Ahmed S
    Mymensingh Med J; 2015 Oct; 24(4):864-7. PubMed ID: 26620033
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An unusual homozygous arylsulfatase: a pseudodeficiency in a metachromatic leukodystrophy Tunisian patient.
    Tinsa F; Caillaud C; Vanier MT; Bousnina D; Boussetta K; Bousnina S
    J Child Neurol; 2010 Jan; 25(1):82-6. PubMed ID: 19574581
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Impaired cerebroside sulfate hydrolysis in fibroblasts of sibs with "pseudo" arylsulfatase A deficiency without metachromatic leukodystrophy.
    Hreidarsson SJ; Thomas GH; Kihara H; Fluharty AL; Kolodny EH; Moser HW; Reynolds LW
    Pediatr Res; 1983 Sep; 17(9):701-4. PubMed ID: 6137805
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of a new Arylsulfatase A (ARSA) gene mutation in Tunisian patients with metachromatic leukodystrophy (MLD).
    Dorboz I; Eymard-Pierre E; Kefi R; Abdelhak S; Miladi N; Boespflug-Tanguy O;
    J Neurol Sci; 2009 Dec; 287(1-2):278-80. PubMed ID: 19699491
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading test.
    Kihara H; Ho CK; Fluharty AL; Tsay KK; Hartlage PL
    Pediatr Res; 1980 Mar; 14(3):224-7. PubMed ID: 6104322
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Biochemical profiling to predict disease severity in metachromatic leukodystrophy.
    Tan MA; Fuller M; Zabidi-Hussin ZA; Hopwood JJ; Meikle PJ
    Mol Genet Metab; 2010 Feb; 99(2):142-8. PubMed ID: 19815439
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiency.
    Hageman AT; Gabreëls FJ; de Jong JG; Gabreëls-Festen AA; van den Berg CJ; van Oost BA; Wevers RA
    Arch Neurol; 1995 Apr; 52(4):408-13. PubMed ID: 7710377
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and biochemical study of 29 Brazilian patients with metachromatic leukodystrophy.
    Artigalás O; Lagranha VL; Saraiva-Pereira ML; Burin MG; Lourenço CM; van der Linden H; Santos ML; Rosemberg S; Steiner CE; Kok F; de Souza CF; Jardim LB; Giugliani R; Schwartz IV
    J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S257-62. PubMed ID: 20596894
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Critical issues for the proper diagnosis of Metachromatic Leukodystrophy.
    Lorioli L; Cesani M; Regis S; Morena F; Grossi S; Fumagalli F; Acquati S; Redaelli D; Pini A; Sessa M; Martino S; Filocamo M; Biffi A
    Gene; 2014 Mar; 537(2):348-51. PubMed ID: 24334127
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? - Chances and challenges.
    Santhanakumaran V; Groeschel S; Harzer K; Kehrer C; Elgün S; Beck-Wödl S; Hengel H; Schöls L; Haack TB; Krägeloh-Mann I; Laugwitz L
    Mol Genet Metab; 2022 Nov; 137(3):273-282. PubMed ID: 36240581
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Demonstration of arylsulfatase A deficiency in metachromatic leukodystrophy and prenatal diagnosis of the disease].
    Tsvetkova IV; Bakharev VA; Kazi Z; Osipova GN; Rozenfel'd EL
    Vopr Med Khim; 1980; 26(4):461-4. PubMed ID: 6109402
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lysosomal leukodystrophies: Krabbe disease and metachromatic leukodystrophy.
    Kohlschütter A
    Handb Clin Neurol; 2013; 113():1611-8. PubMed ID: 23622382
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Metachromatic leukodystrophy without arylsulfatase A deficiency: a new case of saposin-B deficiency.
    Deconinck N; Messaaoui A; Ziereisen F; Kadhim H; Sznajer Y; Pelc K; Nassogne MC; Vanier MT; Dan B
    Eur J Paediatr Neurol; 2008 Jan; 12(1):46-50. PubMed ID: 17616409
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Metachromatic leukodystrophy: report of 2 cases with histochemistry of nerves and muscles].
    Werneck LC; Pereira JL; Bruck I
    Arq Neuropsiquiatr; 1980 Sep; 38(3):237-48. PubMed ID: 6110417
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Metachromatic leukodystrophy caused by a partial cerebroside sulfatase.
    Kihara H; Fluharty AL; O'Brien JS; Fish CH
    Clin Genet; 1982 Apr; 21(4):253-61. PubMed ID: 6125284
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: a new mutation in the ARSA gene.
    Marcão AM; Wiest R; Schindler K; Wiesmann U; Weis J; Schroth G; Miranda MC; Sturzenegger M; Gieselmann V
    Arch Neurol; 2005 Feb; 62(2):309-13. PubMed ID: 15710861
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A variant form of metachromatic leukodystrophy without arylsulfatase deficiency.
    Hahn AF; Gordon BA; Hinton GG; Gilbert JJ
    Ann Neurol; 1982 Jul; 12(1):33-6. PubMed ID: 6126151
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Pathophysiology of sulfatide metabolism in metachromatic leukodystrophy].
    Wiesmann UN
    Bull Schweiz Akad Med Wiss; 1978 Mar; 34(1-3):33-47. PubMed ID: 27269
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Metachromatic leucodystrophy. Clinical, biological, and therapeutic aspects].
    Barboura I; Ferchichi S; Dandana A; Jaidane Z; Ben Khelifa S; Chahed H; Ben Mansour R; Chebel S; Maire I; Miled A
    Ann Biol Clin (Paris); 2010; 68(4):385-91. PubMed ID: 20650733
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of a novel splicing mutation in the ARSA gene in a patient with late-infantile form of metachromatic leukodystrophy.
    Kang DH; Lee DH; Hong YH; Lee ST; Jeon BR; Lee YK; Ki CS; Lee YW
    Korean J Lab Med; 2010 Oct; 30(5):516-20. PubMed ID: 20890085
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.